Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_assertion wasGeneratedBy ECO_0000218 NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_assertion wasDerivedFrom uniprot-20150221 NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_assertion SIO_000772 10852552 NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_assertion evidence source_evidence_curated NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.
- NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_assertion description "[A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243.RAvakenz49EzsUeqv9SsKqLB2if9TmWCoI0zc9JQn5BzU130_provenance.